Package 0121-0653-04

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-0653-04
Digits Only 0121065304
Product NDC 0121-0653
Product ID 0121-0653_4bf945f4-e607-409c-80f5-90195005d6a7
Description

120 mL in 1 BOTTLE, DROPPER (0121-0653-04)

Marketing

Marketing Status
Marketed Since 2010-09-01
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluphenazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4bf945f4-e607-409c-80f5-90195005d6a7", "openfda": {"upc": ["0301210653049"], "unii": ["ZOU145W1XL"], "rxcui": ["861848"], "spl_set_id": ["0860b3f3-3116-40f8-bcb0-e5c47731bdc8"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 mL in 1 BOTTLE, DROPPER (0121-0653-04)", "package_ndc": "0121-0653-04", "marketing_start_date": "20100901"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "0121-0653_4bf945f4-e607-409c-80f5-90195005d6a7", "dosage_form": "SOLUTION, CONCENTRATE", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0121-0653", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA074725", "marketing_category": "ANDA", "marketing_start_date": "20100901", "listing_expiration_date": "20261231"}